Canonical Allele Identifier: CA2579403595

Gene: ALDOB

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101421784del , CM000671.2:g.101421784del	GRCh38
NC_000009.11:g.104184066del , CM000671.1:g.104184066del	GRCh37
NC_000009.10:g.103223887del	NCBI36
NG_012387.1:g.18998del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647789.2:c.*26del MANE Select	ENSP00000497767.1:n.*26del
ENST00000648064.1:c.*26del	ENSP00000497990.1:n.*26del
ENST00000648758.1:c.*26del	ENSP00000497731.1:n.*26del
ENST00000374855.8:c.*26del	ENSP00000363988.4:n.*26del
ENST00000616752.1:c.*133del	ENSP00000481363.1:n.*133del
NM_000035.3:c.*26del	NP_000026.2:n.*26del
NM_000035.4:c.*26del MANE Select	NP_000026.2:n.*26del